Gene: NKX1-1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54729
Gene Symbol: NKX1-1
NKX1-1 		0.010 Biomarker disease BEFREE The KIF1C mutation is associated with a HSP subtype (SPAX2/SAX2) that combines spastic paraplegia and weakness with cerebellar dysfunction. 24319291 2014